Valeant Pharmaceuticals North America LLC recalls Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 921
Recalled November 11, 2015 · FDA recall D-0163-2016 · Valeant Pharmaceuticals North America
Hazard
Failed Dissolution Specifications: Failed 24 month dissolution testing. · FDA Class II
Units
3341 Bottles
Sold at
U.S. Nationwide
Description
Failed Dissolution Specifications: Failed 24 month dissolution testing.
Product
Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 92130. NDC: 68012-495-90.
Manufacturer(s)
Valeant Pharmaceuticals North America LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →